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Allogene Therapeutics

All articles tagged with #allogene therapeutics

Off-the-shelf CAR-T shows potential to delay lymphoma relapse in interim Phase 3 results
biotech1 month ago

Off-the-shelf CAR-T shows potential to delay lymphoma relapse in interim Phase 3 results

Allogene Therapeutics reported interim Phase 3 data for its off-the-shelf CAR-T therapy cema-cel in B-cell lymphoma, showing 58% MRD negativity in treated patients versus 16% in those observed with standard care, a result that could delay or prevent cancer relapse in high-risk patients, though the data are preliminary.

Off-the-shelf CAR-T shows MRD clearance edge in Allogene's ALPHA3 data
healthcarebiotech1 month ago

Off-the-shelf CAR-T shows MRD clearance edge in Allogene's ALPHA3 data

Allogene Therapeutics reports early ALPHA3 data showing its off-the-shelf donor-derived CAR-T therapy cema-cel achieved a 41.6-percentage-point higher minimal residual disease (MRD) clearance at day 45 versus control (7/12 vs 2/12) in lymphoma patients with MRD after initial chemotherapy. Circulating tumor DNA dropped an average 97.7% in cema-cel-treated patients vs a 26.6% rise in control. No cases of cytokine release syndrome or neurotoxicity were observed, and most patients were treated as outpatients. The trial has enrolled just 24 of about 220 planned participants; enrollment is expected to finish by 2027, with event-free survival data due mid-2027 and mid-2028. If results confirm benefit, cema-cel could become the first donor-derived CAR-T therapy to seek FDA approval, potentially reshaping lymphoma treatment access.»

healthcare1 month ago

Off-the-shelf CAR-T cema-cel lights up MRD clearance in first-line LBCL, hinting at MRD-guided consolidation

Allogene Therapeutics reported interim futility data from the ALPHA3 trial in first-line LBCL showing cemacabtagene ansegedleucel (cema-cel) achieved MRD negativity in 58.3% of patients vs 16.7% with observation (a 41.6-point edge), and a median 97.7% drop in plasma ctDNA versus a 26.6% rise. The treatment was well tolerated with no CRS/ICANS/GvHD and most patients managed outpatient; community centers contributed about a third of activity. Enrollment aims for ~220 patients with interim EFS data due mid-2027 and primary EFS in mid-2028, and positive results could support an MRD-guided approach and potential BLA submission.